drug enforcement administration pharmaceutical training seminar · 2016-07-28 · pharmaceutical...

Inventories, Records, & Reports Drug Enforcement Administration Pharmaceutical Training Seminar

Philadelphia , PA April 12-15, 2016

San Antonio , TX April 25-28, 2016

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Office of Diversion Control Mission

Ensuring an adequate and uninterrupted supply for

legitimate medical and scientific purposes

To prevent, detect, and investigate the diversion of controlled substances from legitimate sources

while

Importer

Practitioner

Pharmacy

Distributor

Manufacturer

Patient

The CSA’s Closed System of Distribution

Authority: • Law Controlled Substance Act

United States Code: Title 21 Food & Drugs

• Regulations Code of Federal Regulations

Title 21 Food & Drugs • Policy

Policy response letters, Manuals, Postings Rulemaking published in Federal Register

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Introduction:

• The Law • The Regulations which further define and

clarify the law • The Violation of the law • The Penalties for the violation of the law

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Law: 21 USC § 822 (a) (1)

• Persons Required to Register: • “Every person who manufactures or distributes

any Controlled Substance or List I Chemical or who proposes to engage in ..”

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Law: 21 USC § 822 (a) (2)

• Persons Required to Register: • “Every person who dispenses, or who proposes

to dispense any controlled substance...”

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Law: 21 USC § 827 (a)(3)

• “ every registrant under this (title) manufacturing, distributing, or dispensing a controlled substance…shall maintain, on a current basis, a complete and accurate record of each substance manufactured, received, sold, delivered, or otherwise disposed of …”

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Law: 21 USC 827 (a)(1),(2)

• Inventories: – When registrant first engages in the

manufacture/distribution/dispensing

– Every second year thereafter

– Complete and accurate record of all stocks on hand

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Law: 21 USC § 827 (b)

• Availability of Records: – Contain information and be in a form as required

by regulation. – Be in a form that is Readily Retrievable. – Be kept and available for Two years.

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Law: 21 USC § 827 (d)

• Periodic Reports Every Manufacturer…at such time…and in such form as the Attorney General may require, make periodic reports to the Attorney General of every sale, delivery, or other disposal by him of any controlled substance, and each distributor shall make such reports...

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Law: 21 USC § 827 (g)

• Every registrant under this subchapter shall be required to report any change of professional or business address in such manner as the Attorney General shall by regulation require.

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Scheduled Investigations

Security Requirements

Recordkeeping Requirements

ARCOS

Established Quotas

Registration

Established Schedules

Maintaining the CSA’s Closed System of Distribution

INVENTORIES

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Inventories: 21 C.F.R. § 1304.11(a)

• Inventory Requirements: – Complete and accurate record – All substances “On Hand” (In possession and

under the control of registrant) – On the date the inventory is taken – Maintained in written, typewritten, or printed form

at the registered location.

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Separate Inventories: 21 C.F.R.§1304.11(a)

• Separate inventories for each Registered Location.

• May be taken: (BOB) Beginning of Business (COB) Close of Business

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Separate Inventories: 21 C.F.R. § 1304.11 (a)

• Separate inventories for each Independent

Activity.

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Initial Inventory Date: 21 C.F.R. § 1304.11 (b)

• Inventory of all Stocks of CS

– On The Date: First Engages in the manufacture, distribution, or dispensing of controlled substances

– Should Be Labeled “Initial Inventory”

– Nothing on Hand: Record “0”

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Biennial Inventory Date: 21 C.F.R.§ 1304.11(c)

• After the Initial Inventory – New Inventory at least Every Two Years – On any date which is within two years of the

previous Biennial Inventory date – Should be labeled “Biennial Inventory” – Nothing on hand: Record “0”

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Newly Controlled Substances: 21 C.F.R. § 1304.11 (d)

• For any newly Controlled Substance – Inventory of all stocks on hand

– On the effective date of the rule

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Inventories: 21 C.F.R. § 1304.11(e)

(1) Inventories for Manufacturers (2) Inventories for Distributors (3) Inventories for Dispensers & Researchers (4) Inventories for Importers & Exporters (5) Inventories for Chemical Analysts

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Inventories (Summary):

• Initial Inventory

• Biennial Inventory

• Newly Controlled Drugs

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RECORDS

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Records: 21 C.F.R. § 1304.21(a)

• Maintain on a Current Basis... – Complete and Accurate record of each

substance…Manufactured, Imported, Exported, Received, Sold, Delivered, or otherwise disposed of ...

– Except No registrant is required to maintain a Perpetual Inventory

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Separate Records: 21 C.F.R. § 1304.04(f)(1); (g); (h)(1)

• Schedule I & II:

– Maintained Separately from all other records

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• Schedules III, IV, & V – Separate from All Other Records

• or “Readily Retrievable” – Separated out from all other records in a

reasonable time period – CS Items asterisk, redlined, or in some manner

which sets them visually apart – Red letter “C” lower right corner

Separate Records: 21 C.F.R.§ 1304.04 (f)(2); (g); (h)(2)

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Separate Records: 21 C.F.R. § 1304.21(b)

• Separate Records.. For each Registered

Location.

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Separate Records: 21 C.F.R. § 1304.21(c)

• Separate Records.. For each Independent

Activity for which he/she is registered.

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Dates for Records: 21 C.F.R. § 1304.21(d)

• Dates must be the Actual Date of transfer

(Received, Imported, Exported, Distributed, or otherwise Transferred, etc.)

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Records: 21 C.F.R. § 1304.22

• Manufacturers – Bulk Form – In-Process – Finished Goods

• Distributors • Importers/Exporters • Dispensers/Researchers/Opioid Treatment

Programs

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Records: (Distributors) 21 C.F.R. § 1304.22(b)

• Records for Distributors – Maintain Records with the same information

required of manufacturers pursuant to (a)(2), (i), (ii), (iv), (vii), (viii), and (ix) of this section.

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Records: (Distributors) 21 C.F.R. § 1304.22(b)

• Records for Distributors –Name of CS –Finished Form –# of Containers –# of Units Distributed –Name, Address, and DEA# from whom

received or to whom distributed.

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Records: (Dispenser/Research) 21 C.F.R. § 1304.22(c)

• Shall maintain records with the same

information required of manufacturers pursuant to paragraph (a)(2)(i), (ii), (iv), (vii), and (ix) of this section.

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Records: 21 C.F.R. § 1304.22(c)

• Records for Dispensers and Researchers: – Name of CS, Form, Quantity, Strength – Number of Units or Volume of Finished Form

dispensed – Name, address of the person to whom it was

dispensed – Date of dispensing

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Records: 21 C.F.R. § 1304.22(c)

• Records for Dispensers and Researchers – Written or typewritten name or initials of the

individual who dispensed or administered the substance on behalf of the dispenser

– Amount disposed of in any other manner

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Records: 21 C.F.R. § 1312.12

• Records for Importers • Application for Permit: DEA 357 • Import Permit: (DEA 35) • Schedule I, II • Narcotic Substance (CIII, CIV, or CV) • Non-Narcotic (CIV, CV) which is also

listed in Schedule I or II of the International Psychotropic Convention 36

Records: 21 C.F.R. §1312.18(b)

• Records for Importers • Import Declaration

– DEA 236 – Non-Narcotic Substance (CIII, CIV, CV) – Submit 15 Days Before Importation

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Records: 21 C.F.R.§ 1312.21/22

• Records for Exporters • Application for Permit: DEA 161, DEA 161R • Export Permit: DEA 36

– Schedule I, II – Narcotic Substance (CIII, CIV) – Non-Narcotic (CIV, CV) which is also listed in

Schedule I or II of the Convention of Psychotropic Substances

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Records : 21 C.F.R. § 1312.27

• Records for Exporters • Export Declaration

– DEA 236 – Non-Narcotic Substance (CIII, CIV, CV) – Narcotic Substances (CV)

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Import Export Online Submission

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Records : 21 C.F.R. § 1304.23

• Records for Chemical Analysts

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Order Forms: 21 C.F.R. §1305

• Order Forms are required for each transfer of a CS in Schedule I & II except…: – Distributions to persons exempt from registration – Exports from the U.S. – Deliveries to …analytical laboratory – Deliveries from a central fill pharmacy…to a retail

pharmacy

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Order Forms: 21 C.F.R. § 1305

• Obtaining Order Forms: – Order Forms are Issued in Books of

Seven Forms Each.

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• Obtaining Order Forms: – Each Form has three copies:

• Supplier • DEA • Purchaser

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• Obtaining Order Forms: – Order Forms are serially numbered and issued with – Name – Address – Registration # of the Registrant – Authorized activity and schedules of the registrant

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• Executing Order Forms: – Purchaser must prepare and execute …in

triplicate by means of interleaved …sheets – Each form has three parts… – Each form has ten lines – Only one item per line – Total # of items are noted on form

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• Executing Order Forms: – Prepared and executed by the purchaser in

triplicate. – Prepared by use of a typewriter, pen, or indelible

pencil. – Signature should be legible. – Attachments to order forms will not be used.

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• Executing Order Forms: – Name and address of the supplier from whom the

CS are being ordered shall be entered on the form. – Only one supplier may be listed on any one form.

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• Executing Order Forms: – An order form may be executed only on behalf of

the Registrant name on the form. – And only if his Registration has not expired, been

revoked, or suspended. – Each order form shall be dated and signed by a

person authorized to sign an application for registration.

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• Executing Order Forms: – This may be the person who signed the original

application – Or by a person to whom he gave Power of

Attorney.

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• Executing Order Forms:

– The Power of Attorney must be signed by: • the person who signed the most recent application; • the person to whom the power of attorney is being

granted; • and two witnesses.

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• Executing Order Forms: – The Power of Attorney must be filed with the

Executed Order Forms of the purchaser. – The Power of Attorney must be available for

inspection along with other order records.


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• Executing Order Forms: – A Power of Attorney must be revoked by the

person who signed the most recent application for DEA registration or re-registration, and two witnesses.

– DEA does not print Power of Attorney or Notice of Revocation Forms.

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• Filling Order Forms: – The Purchaser must Submit Copy 1 and copy 2 of

the Order Form to the supplier and retain copy 3 in (their) Files.

– The supplier must fill the entire order, if possible and the supplier desires to do so, and must record on Copies 1 and 2 the number of commercial or bulk containers furnished on each item and the date on which such containers are shipped.


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• Filling Order Forms: – If an order cannot be filled in it’s entirety, it may

be filled in part and the balance supplied by additional shipments within 60 days following the date of the order form.

– No order form is valid more than 60 days after its execution by the purchaser.

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• Filling Order Forms: – The supplier must retain Copy 1 of the order

form for his own files and forward Copy 2 to the DEA office in the region where the supplier is located.

– Copy 2 must be forwarded at the close of the month during which the final shipment is made or the 60 day validity period expires.


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• Filling Order Forms: – The purchaser must record on Copy 3 of the order

form the number of commercial or bulk containers furnished on each item and the dates on which such containers are received by the purchaser.

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• Unaccepted Order Forms: – No order form shall be filled if : – The order is not complete, legible or properly

prepared, executed or endorsed or shows any alteration, erasure or change of description.

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• Unaccepted Order Forms: – A defective order form may not be corrected; it

must be replaced by a new order form.

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• Preservation of Order Forms: – Order forms must be maintained separately from

all other records of the registrant. – They are required to be kept available for

inspection for a period of two years.

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What is the Controlled Substance Ordering System (CSOS)?

• DEA Form 222 in Electronic Form • “Electronic DEA Form 222” • May include C/S’s that are not in

schedule I & II and non-controlled substances

What is CSOS? • Is a Voluntary option for ordering controlled

substances (C/S’s) • A means by which a DEA registrant is able to

order C/S’s in a secure electronic environment.

• In addition to the DEA Form-222, Official Paper Order Form.

• If you understand the paper process, you will understand the electronic process.

CSOS Technical Matters

• In order for CSOS to work it must provide: – Authentication: must positively verify the

signer – Non-repudiation: strong and substantial

evidence of the sender’s identity, and – Message Integrity: must determine whether

the contents of the order have been altered in transmission.

Who Can Participate in CSOS? • Any DEA registrant (Purchaser) who is

authorized by law to handle C/S’s may participate in CSOS.

• Any DEA registrant (Supplier) who is authorized by law to manufacture and/or distribute C/S’s may fill CSOS orders. – Manufacturers, Distributors, etc.

How Does CSOS Work? • To participate the purchaser must be a

DEA registrant • DEA is the Certificate Authority

– Verifies the authenticity of a person requesting a digital certificate,

– Issues, renews, and revokes digital certificates,

– Maintains a Certificate Revocation Listing.

How Does CSOS Work? • The DEA registrant completes the CSOS

application, • Acknowledges the User Agreement • Provides two government picture ID’s • Notary authenticates the individual and

ID’s • DEA verifies the application, current

registration, and supporting documents.

How Does CSOS Work?

• DEA approves and issues a digital certificate in two parts; – The first part is mailed via the U.S. Postal Service

with the User Agreement. – The second part is transmitted via e-mail – Upon receipt of both parts, combined, they activate

the uniquely assigned digital certificate.

How Does CSOS Work?

• The issued digital certificate can be used only by the person to whom it assigned. In essence, it is their wet ink signature.

• In placing an order, the purchaser, utilizing their User ID and Password together, activates the digital certificate.

21 C.F.R. § 1305.21(b) Requirements for Electronic Orders

• A CSOS Order must contain: – A unique number of 9 characters; last two digits

of the year, an “X”, and six unique characters, (pre-printed on DEA Form-222)

– Purchasers DEA registration number, – Name of Supplier, – Complete address of the supplier, – Suppliers DEA registration number,

21 C.F.R. § 1305.21(b) Requirements for Electronic Orders

– Date order was signed, – Name and strength of the C/S being ordered,

• The NDC number may be completed by either the purchaser or supplier

– The package size (e.g. Bottle of 100), – The quantity ordered (e.g. 5 Bottles),

21 C.F.R. § 1305.22(c) Procedure for Filling Electronic Orders

• The supplier must: – Verify the integrity of the order using Public

Key Infrastructure (PKI) – Verify the digital certificate has not expired, – Validate the digital certificate against the

Certificate Revocation Listing (CRL) – Validate the registrant is authorized to order

C/S’s

21 C.F.R. § 1305.25 Unaccepted and Defective Electronic Orders

• A supplier cannot fill any order if: – Required data fields are not complete, – The order is not digitally signed, – The digital certificate has expired or is revoked, – Validation process is invalid for any reason,

Comparison of CSOS & Paper DEA Form 222 Order Form

• Must be digitally signed.

• Required fields must be completed

• Coordinator must delegate in writing for others to sign.

• Supplier must be designated.

• Must be signed (original signature)

• Required fields and limited lines must be completed.

• Power of Attorney for other to sign.

• Supplier must be designated.

Comparison of CSOS & Paper DEA Form 222 Order Form

• Must retain for two years.

• Records must be readily retrievable.

• Records must be easily readable.

• All associated records must be linked to the original order.

• Must retain for two years.

• Records must be readily retrievable.

Seller’s Requirements

• Must electronically retain all orders for two years • All associated records must be linked to the

archived CSOS order. • All CSOS orders must be readily retrievable. • All CSOS orders must be reported to DEA within

two business days of being filled. • All CSOS orders must be rendered into a format

that can be easily readable. • CSOS reports must also be reported to ARCOS.

Purchaser’s Requirements • Must electronically retain all CSOS

orders for two years. • All associated records must be linked to

the original archived CSOS order. • All CSOS records must be readily

retrievable. • All CSOS records must be rendered to a

format that is easily readable

Purchaser’s Requirements § Must maintain a copy of the User

Agreement on file. § Must report any suspected or actual

compromise of any digital certificate. § Cannot share or authorize use of their

digital signature to any other person § Must protect their password, etc.

REPORTS

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Destruction of CS: 21 C.F.R. § 1307.21

• Destruction of Controlled Substances – If a Registrant:

• DEA Form 41 - Three Copies

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Destruction of CS: 21 C.F.R. § 1307.21

• If not a Registrant: – Letter – Name and Address of Person – Name & Quantity of All Substances to Be

Disposed of – How the person obtained the substance, if known;

and name, address, and registration number…of person who possessed (it) prior

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Reports to ARCOS : 21 C.F.R. § 1304.33

• Automated Reports & Consolidated Ordering System

• Who Must Report? -Manufacturers (All) -Distributors (Including Reverse Distributors)

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Reports to ARCOS: 21 C.F.R.§ 1304.33

• What Must They Report? – Acquisition/Distribution of:

• Schedule I & II • Narcotics in Schedule I • GHB drug products in Schedule III • Selected psychotropic substances in Schedules III & IV

(Manufacturers only)

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Reports to ARCOS: 21 C.F.R. § 1304.33

• When – Every Quarter: No Later Than the 15th – All Stocks of CS on Hand as of COB 12/31

• How Must They Report? – On-line Reporting – Or DEA Form 333

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Suspicious Orders : 21 C.F.R.§ 1301.74 (b)

• The registrant shall design and operate a system to disclose to the registrant suspicious orders of controlled substances. The registrant shall inform the Field Division Office …in his area of suspicious orders when discovered by the registrant.

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• Suspicious Orders Include: – Orders of Unusual Size – Orders Deviating Substantially From a normal

pattern – Orders of Unusual Frequency

Suspicious Orders

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Reporting the Theft or Loss of Controlled Substances

Paper or Online Submission

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21 C.F.R. § 1301.74(c), 1301.76(b)

• The registrant shall notify the Field Division Office of the Administration in his area of any theft or significant loss of any controlled substances within one business day of discovery.

• The registrant shall also complete, and submit DEA Form 106…

• “Significant Loss” is also defined here.

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21 C.F.R. § 1301.74(c), 1301.76(e)

• The supplier shall be responsible for reporting in-transit losses of controlled substances by the common or contract carrier selected pursuant to paragraph (e) of this section within one business day of discovery of such theft or loss.

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Theft/Loss of CS (DEA 106) : 21 C.F.R. § 1301.74 (c), 1301.76 (b)

• The registrant shall also complete DEA Form 106 regarding such theft or loss. – Theft should be reported to local police with

jurisdiction where the theft occurred. – Theft should also be reported to any state agency

which requires such reports.

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21 C.F.R. § 1301.74(c)

• Thefts and significant losses must be reported whether or not the controlled substances are subsequently recovered and/or the responsible parties are identified and action taken against them.

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Theft or Loss Defined

• Actual Theft or Loss • Not an Inventory Adjustment (not for

balancing inventory) • Loss (Unexplained Disappearance). • Any discovered shortage which the firm

cannot convincingly establish to have been diverted after reasonable review/ investigation should generally be considered as a reportable loss.

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Theft or Loss Defined

• Does not include Breakage, Damage, and/or Spillage which is still recoverable.

• Options (for Recoverable Substances): – DEA 41- Permission to Destroy – Reverse Distributor

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DEA POLICY: Who Should Report?

• In-Transit Losses: Supplier • As soon as the registrant signs for the (accepts)

shipment it becomes the responsibility of the purchaser to report any thefts or losses.

• If the purchaser does not sign for (accept) the shipment it is the responsibility of the shipper to report the theft/loss of the material.

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Contact Information: Abby Hayes, Acting Unit Chief Regulatory Unit/ODGR Drug Enforcement Administration 8701 Morrissette Drive Springfield, Virginia 22152 202-307-8910 (Office) 202-307-8101 (Fax) [email protected]

drug enforcement administration pharmaceutical training seminar · 2016-07-28 · pharmaceutical...

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